Copy-number variation — deleted or duplicated regions of DNA — is widespread in the human genome. A systematic population survey of the common variants provides an invaluable resource for further studies.
References
Conrad, D. F. et al. Nature doi:10.1038/nature08516 (2009). | Article
Iafrate, A. J. et al. Nature Genet. 36, 949–951 (2004).
Redon, R. et al. Nature 444, 444–454 (2006).
Korbel, J. O. et al. Science 318, 420–426 (2007).
Kidd, J. M. et al. Nature 453, 56–64 (2008).
The Wellcome Trust Case Control Consortium Nature 447, 661–678 (2007).
McCarroll, S. A. et al. Nature Genet. 40, 1107–1112 (2008).
de Cid, R. et al. Nature Genet. 41, 211–215 (2009).
Willer, C. J. et al. Nature Genet. 41, 25–34 (2009). | Article
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Armour, J. Sharp focus on the variable genome. Nature 461, 735–736 (2009). https://doi.org/10.1038/461735a
Published:
Issue Date:
DOI: https://doi.org/10.1038/461735a
- Springer Nature Limited
This article is cited by
-
Sexes, species, and genomes: why males and females are not like humans and chimpanzees
Biology & Philosophy (2010)