Q.51

A variable number of tandem repeats (VNTR) locus has 15 different alleles. The number of genotypes possible in a population for this VNTR is ________.

Introduction

In genetics, understanding VNTR locus 15 alleles genotypes is crucial for DNA profiling and competitive exams like CSIR NET. A Variable Number of Tandem Repeats (VNTR) locus with 15 different alleles produces exactly 120 possible genotypes in a population, calculated via standard combinatorial genetics [memory:1].

VNTR Basics

Variable Number Tandem Repeats (VNTRs) are DNA regions with short sequences repeated multiple times in tandem, varying in repeat number across individuals, creating distinct alleles. Each allele differs by repeat count, making VNTRs useful in genetics for DNA fingerprinting and population studies. In diploid organisms like humans, individuals inherit one allele per chromosome at a locus, forming genotypes from allele pairs [conversation_history:10].

Genotype Calculation

Genotypes include homozygous (identical alleles, like A1/A1) and heterozygous (different alleles, like A1/A2) forms.

Homozygous genotypes = allele count = 15
Heterozygous genotypes = n(n−1)/2 = 15×14/2 = 105

Total Genotypes: 15 + 105 = 120
Direct formula: n(n+1)/2 = 15×16/2 = 120 [memory:2].

Step-by-Step Calculation

Homozygous Genotypes

  • One per allele (A1/A1 to A15/A15)
  • Total = 15

Heterozygous Genotypes

  • Unique pairs without regard to order
  • Combinations: 15×14/2 = 105

Total Genotypes

15 (homozygous) + 105 (heterozygous) = 120

Common Errors to Avoid

❌ Mistake 1: 15² = 225 (ignores unordered pairs)
❌ Mistake 2: 15×14 = 210 (permutations, not combinations)
✅ Correct: 15(15+1)/2 = 120

Applications in Genetics

VNTR analysis supports biodiversity studies and disease mapping due to extensive allelic diversity. These hypervariable loci enable high-resolution genotyping for forensics and paternity testing [conversation_history:10].

💡 CSIR NET Tip: Master this combinatorial formula for the Molecular Genetics section. Questions often test understanding of unordered pairs in diploid genotypes [memory:1].

 

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