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IGCSE · Cambridge (CIE) · 0610

Investigate invented ABO phenotype counts without inferring population genotypes

Categorical counts need a total, clear labels and a stated sample.

Variation pathway · 18.1

Core and Extended; Biology 0610, 2026–2028. Use the stated specimen features and evidence. Diagrams are schematic. Written practice is self-checked

Before you begin

  • Recall genes, alleles, genotype and phenotype from the inheritance pathway. Use the stated organism, units and sample; the records in these lessons are invented.

Work on paper. Try each question before revealing help, and explain why your method works.

Quick readiness check

What denominator gives a sample phenotype percentage?

What you will learn

  • Describe a discontinuous sample distribution
  • Calculate labelled phenotype frequencies with evidence limits

Original teaching model. Measurements, categories, DNA fragments and comparison records are invented; assumptions and sample boundaries are stated.

Investigate invented ABO phenotype counts without inferring population genotypesSixty invented phenotype records, not clinical data or population-wide frequencies.Invented ABO phenotype recordsVertical scale: valid phenotypecount2424A1818B66AB1212OSample total: 60Counts describe these inventedrecords, not an entire population
Sixty invented phenotype records, not clinical data or population-wide frequencies.
Variation measurement and evidence key
FeatureMeaning
Total records60 fictional phenotypes
CountsA 24 / B 18 / AB 6 / O 12
Percentages40% / 30% / 10% / 20%
Inference limitSample phenotype counts do not identify all genotypes

Describe a discontinuous sample distribution

The original anonymised teaching dataset contains sixty invented ABO phenotype records: twenty-four A, eighteen B, six AB and twelve O. These are fictional data, not student medical results or a recommendation to test anyone’s blood. The common-model categories are distinct, so a bar chart gives each category a labelled bar with a gap between it and the next category. The horizontal order is a presentation choice rather than a continuous biological scale.

Add the counts to check the sample denominator: twenty-four plus eighteen plus six plus twelve equals sixty. A phenotype percentage is its count divided by sixty times one hundred. This gives A forty per cent, B thirty per cent, AB ten per cent and O twenty per cent. The counts sum to sixty and the percentages sum to one hundred, which checks the arithmetic but does not prove that the sample represents a wider population.

Calculate labelled phenotype frequencies with evidence limits

A is the most frequent phenotype in these records. That statement concerns the sample, not every region or age group. A sample intentionally selected to include particular groups can distort an estimate of a population distribution. The supplied phenotype counts also do not identify all genotypes: A could correspond to IAIA or IAIo and B to IBIB or IBIo in the common inheritance model.

Investigate discontinuous variation by classifying a supplied safe record set with a defined key, tallying each valid record once and describing the category frequencies. Do not average the arbitrary category names or interpret the four bars as body measurements. A separate genotype investigation would require appropriate additional evidence. Written handling of invented records is not clinical testing, consent for private data collection or supervised practical certification.

Pause and explain

Can the 24 A phenotype records all be identified as IAIA from these counts alone?

Put the idea to work

Worked example

Calculate the proportion of phenotype AB in the sixty invented records.

Show the worked solution
  1. The AB count is 6 and the checked total is 24 + 18 + 6 + 12 = 60.
  2. Compute 6/60 × 100 = 10%.

Answer AB represents 10% of the invented sample; this does not establish a population-wide frequency.

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From guided practice to a new situation

Write your answer and reasoning first. Use a hint only if you are stuck. The model solution is for self-checking; your written work is not automatically marked.

1 · Guided

Find the percentages of A and AB in the supplied sixty-record sample.

Give me a hint

Divide each count by the same checked total.

Compare my reasoning
  1. Calculate 24/60 × 100 for A.
  2. Calculate 6/60 × 100 for AB.

A is 40% and AB is 10% of this invented sample.

Look for these in your work

  • Same 60-record denominator
  • Both percentages labelled
2 · Independent

Find the B and O percentages, then check all four percentages sum correctly.

Give me a hint

Use counts 18 and 12 with the total 60.

Compare my reasoning
  1. B = 18/60 × 100 = 30%; O = 12/60 × 100 = 20%.
  2. Combine with A 40% and AB 10% to obtain 100%.

B 30%, O 20%; all four sum to 100%.

Look for these in your work

  • Correct B and O arithmetic
  • Total percentage check
3 · Transfer

A researcher selects exactly sixty fictional records to obtain this chart and claims it proves regional ABO frequencies and every A genotype. Evaluate both claims.

Give me a hint

Sampling and phenotype ambiguity are different limits.

Compare my reasoning
  1. A selected record set need not represent the region.
  2. A phenotype can be IAIA or IAIo in the common model.

Neither claim follows: the chart describes its invented sample, and A phenotype counts cannot distinguish the two common A genotypes.

Look for these in your work

  • Sampling limit
  • Genotype ambiguity

Common mistakes

  • Using only two categories in the denominator
  • Inferring IAIA from every A phenotype
  • Treating invented data as medical records
Recall without your notes

What can you explain now?

Can the 24 A phenotype records all be identified as IAIA from these counts alone?

Compare with the explanation

No; A also permits IAIo

Phenotype counts leave common-model genotype ambiguity.

After trying it yourself, choose your next review. This is your self-assessment.

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Make it stick

Without your notes, describe a discontinuous sample distribution and calculate labelled phenotype frequencies with evidence limits. Keep units, the stated sample and the limits of the evidence clear.

If you needed the solution, close it and solve the problem again from a blank page. A correct answer is stronger when you can explain the reason for each step.

Keep learning Biology

Course scope and assessment

780 sequenced lessons provide 2340 guided, independent and application problems in characteristics, classification, cells, organisation, specimen size, membrane transport, biological molecules, enzymes, plant and human nutrition, plant transport, circulatory systems, the heart, blood vessels, blood, disease transmission, body defences, immunity, gas exchange in humans, respiration energy uses and investigations, aerobic respiration, anaerobic respiration and recovery, excretion in humans, coordination and response, sense organs, hormones, homeostasis, tropic responses, drugs, asexual reproduction, sexual reproduction, sexual reproduction in plants, sexual reproduction in humans, sex hormones in humans, sexually transmitted infections, chromosomes, genes and proteins, mitosis, meiosis, monohybrid inheritance, variation, adaptive features, selection, energy flow, food chains and webs, nutrient cycles, population, community, ecosystem, population-growth phases, food supply, habitat destruction, pollution, conservation, biotechnology and genetic modification. 61 of 61 syllabus sections have linked teaching and staged practice. The earlier inheritance overview remains introductory, and the monohybrid pathway develops the relevant Core and Supplement requirements. This is not full programme completion or guaranteed exam readiness. Written practice is self-checked.

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