Article

The functional impact of copy number variation in the human genome

2012-01-01

Abstract excerpt

Copy number variation (CNV) is a class of genetic variation where large segments of the genome vary in copy number among different individuals. It has become clear in the past decade that CNV affects a significant proportion of the human genome and can play an important role in human disease. With array-based copy number detection and the current generation of sequencing technologies, our ability to discover genet...

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Literature Corpus work: 65e6f9f5-c61a-5b87-aa41-0db94b0ddc66
DOI: 10.17863/cam.16350

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