TABLE 2 

From the following article:

Origins and functional impact of copy number variation in the human genome

Donald F. Conrad, Dalila Pinto, Richard Redon, Lars Feuk, Omer Gokcumen, Yujun Zhang, Jan Aerts, T. Daniel Andrews, Chris Barnes, Peter Campbell, Tomas Fitzgerald, Min Hu, Chun Hwa Ihm, Kati Kristiansson, Daniel G. MacArthur, Jeffrey R. MacDonald, Ifejinelo Onyiah, Andy Wing Chun Pang, Sam Robson, Kathy Stirrups, Armand Valsesia, Klaudia Walter, John Wei, The Wellcome Trust Case Control Consortium, Chris Tyler-Smith, Nigel P. Carter, Charles Lee, Stephen W. Scherer & Matthew E. Hurles

Nature 464, 704-712(1 April 2010)

doi:10.1038/nature08516

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Table 2. Trait-associated SNPs with possible causal CNVs.