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Multiple Choice
Which of the following genomic variation refers to different number of gene copies between individuals and populations?
A
Single nucleotide polymorphisms
B
Copy number variants
C
CA Repeats
D
Transposons
Verified step by step guidance
1
Understand the concept of genomic variation: Genomic variation refers to differences in the DNA sequence among individuals. These variations can occur in different forms, such as single nucleotide polymorphisms (SNPs), copy number variants (CNVs), and others.
Define single nucleotide polymorphisms (SNPs): SNPs are variations at a single position in a DNA sequence among individuals. They are the most common type of genetic variation and usually do not involve changes in the number of gene copies.
Define copy number variants (CNVs): CNVs are a type of structural variation where the number of copies of a particular gene or genomic region varies between individuals. This can result in duplications or deletions of large sections of DNA, affecting gene dosage and potentially leading to phenotypic differences.
Define CA repeats: CA repeats, also known as microsatellites, are short, repetitive sequences of DNA. They are highly polymorphic and can vary in length between individuals, but they do not typically involve changes in the number of gene copies.
Define transposons: Transposons, or 'jumping genes,' are DNA sequences that can change their position within the genome. While they can cause mutations and genomic rearrangements, they are not primarily associated with variations in gene copy number.