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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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| Main Authors: | , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2010
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| Assuntos: | |
| Acesso em linha: | 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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