Copy-number variations (CNVs) are chromosomal mutations that are always due to duplications.
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Q117: Which copy-number variation (CNV) is MOST likely
Q118: Which one of the following measures has
Q119: Would you consider the SNP associated with
Q120: Gel electrophoresis is the preferred method for
Q121: SNPs arise from:
A)deletions.
B)inversions.
C)translocations.
D)duplications.
E)point mutations.
Q123: CNV stands for:
A)copy-number variation.
B)central nucleotide variant.
C)copy nucleotide
Q124: The biggest difference between copy-number variation (CNV)
Q125: A newly arisen point mutation always creates
Q126: The lethality of most monosomies and trisomies
Q127: The difference between a single-nucleotide polymorphism (SNP)
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