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Genome-wide association study of copy number variation in 16,000 cases of eight common diseases and 3,000 shared controls
Copy number variants (CNVs) account for a major proportion of human genetic polymorphism and have been predicted to play an important role in genetic susceptibility to common disease. To address this we undertook a large direct genome-wide study of association between CNVs and eight common human dis...
| Formato: | Texto |
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| Lenguaje: | English |
| Publicado: |
2010
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2892339/ https://www.ncbi.nlm.nih.gov/pubmed/20360734 http://dx.doi.org/10.1038/nature08979 |