Article
SgD-CNV, a database for common and rare copy number variants in three Asian populations.
Human mutation - 1 Dec 2011
Xu Haiyan, Poh Wan-Ting, Sim Xueling, Ong Rick Twee-Hee, Suo Chen, Tay Wan-Ting, Khor Chiea-Chuen, Seielstad Mark, Liu Jianjun, Aung Tin, Tai E-Shyong, Wong Tien-Yin, Chia Kee-Seng, Teo Yik-Ying
Abstract excerpt
Copy number variants (CNVs) extend our understanding of the genetic diversity in humans. However, the distribution and characteristics of CNVs in Asian populations remain largely unexplored, especially for rare CNVs that have emerged as important genetic factors for complex traits. In the present study, we performed an in-depth investigation of common and rare CNVs across 8,148 individuals from the three major...
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