Novel population specific autosomal copy number variation and its functional analysis amongst Negritos from Peninsular Malaysia
Copy number variation (CNV) has been recognized as a major contributor to human genome diversity. It plays an important role in determining phenotypes and has been associated with a number of common and complex diseases. However CNV data from diverse populations is still limited. Here we report the...
| Published in: | PLoS ONE |
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| Main Author: | |
| Format: | Article |
| Language: | English |
| Published: |
Public Library of Science
2014
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| Online Access: | https://www.scopus.com/inward/record.uri?eid=2-s2.0-84903535290&doi=10.1371%2fjournal.pone.0100371&partnerID=40&md5=39eddc93b0c5bd7444c89b9e0ff9a1c2 |