Population-genetic nature of copy number variations in the human genome

Copy number variations (CNVs) are universal genetic variations, and their association with disease has been increasingly recognized. We designed high-density microarrays for CNVs, and detected 3000–4000 CNVs (4–6% of the genomic sequence) per population that included CNVs previously missed because o...

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Päätekijät: Kato, Mamoru, Kawaguchi, Takahisa, Ishikawa, Shumpei, Umeda, Takayoshi, Nakamichi, Reiichiro, Shapero, Michael H., Jones, Keith W., Nakamura, Yusuke, Aburatani, Hiroyuki, Tsunoda, Tatsuhiko
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Oxford University Press 2010
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Articles
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC2816609/
https://ncbi.nlm.nih.gov/pubmed/19966329
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddp541
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