Article

Intronic CNVs cause gene expression variation in human populations

2017-08-01

Abstract excerpt

Introns can be extraordinarily large and they account for the majority of the DNA sequence in human genes. However, little is known about their population patterns of structural variation and their functional implication. By combining the most extensive maps of CNVs in human populations, we have found that intronic losses are the most frequent copy number variants (CNVs) in protein-coding genes in human, with more...

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Literature Corpus work: ee82839b-49e8-5a2c-955b-0bd5dc8ea6d3
DOI: 10.1101/171165

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