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...

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Bibliographic Details
Published in:PLoS ONE
Main Author: Mokhtar S.S.; Marshall C.R.; Phipps M.E.; Thiruvahindrapuram B.; Lionel A.C.; Scherer S.W.; Peng H.B.
Format: Article
Language:English
Published: Public Library of Science 2014
Online Access:https://www.scopus.com/inward/record.uri?eid=2-s2.0-84903535290&doi=10.1371%2fjournal.pone.0100371&partnerID=40&md5=39eddc93b0c5bd7444c89b9e0ff9a1c2

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