Related Experiment Video

Updated: Aug 29, 2026

Array Comparative Genomic Hybridization (Array CGH) for Detection of Genomic Copy Number Variants
09:16

Array Comparative Genomic Hybridization (Array CGH) for Detection of Genomic Copy Number Variants

Published on: February 21, 2015

Use of complete coverage array comparative genomic hybridization to define copy number alterations on chromosome 3p

Cathie Garnis1, Corisande Baldwin, Lewei Zhang

  • 1British Columbia Cancer Research Centre, Vancouver, British Columbia, Canada. cgarnis@bccrc.ca

Cancer Research
|December 26, 2003
PubMed

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Comparing Copy Number Variations and SNPs02:26

Comparing Copy Number Variations and SNPs

Sequencing of the human genome has opened up several best-kept secrets of the genome. Scientists have identified thousands of genome variations that exist within a population. These variations can be a single nucleotide or a larger chromosomal variation.
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...