Copy number variation in the human Y chromosome in the UK population

We have assessed copy number variation (CNV) in the male-specific part of the human Y chromosome discovered by array comparative genomic hybridization (array-CGH) in 411 apparently healthy UK males, and validated the findings using SNP genotype intensity data available for 149 of them. After manual...

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Detalhes bibliográficos
Publicado no:Hum Genet
Main Authors: Wei, Wei, Fitzgerald, Tomas, Ayub, Qasim, Massaia, Andrea, Smith, Blair B., Dominiczak, Anna A., Morris, Andrew A., Porteous, David D., Hurles, Matthew E., Tyler-Smith, Chris, Xue, Yali
Formato: Artigo
Idioma:Inglês
Publicado em: Springer Berlin Heidelberg 2015
Assuntos:
Original Investigation
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4460274/
https://ncbi.nlm.nih.gov/pubmed/25957587
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00439-015-1562-5
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