Format

Send to

Choose Destination
See comment in PubMed Commons below
Nat Genet. 2010 May;42(5):365-6. doi: 10.1038/ng0510-365.

Copy number variation and human genome maps.

Author information

1
Department of Genetics, Harvard Medical School, Boston, Massachusetts, USA. mccarroll@genetics.med.harvard.edu

Abstract

Maps of human genome copy number variation (CNV) are maturing into useful resources for complex disease genetics. Four new studies increase the resolution of CNV maps and seek to locate human phenotypic variation on these maps.

PMID:
20428091
DOI:
10.1038/ng0510-365
[Indexed for MEDLINE]
PubMed Commons home

PubMed Commons

0 comments
How to join PubMed Commons

    Supplemental Content

    Full text links

    Icon for Nature Publishing Group
    Loading ...
    Support Center