Microarray-based maps of copy-number variant regions in European and sub-Saharan populations.
The genetic basis of phenotypic variation can be partially explained by the presence of copy-number variations (CNVs). Currently available methods for CNV assessment include high-density single-nucleotide polymorphism (SNP) microarrays that have become an indispensable tool in genome-wide associatio...
Main Authors: | Christian Vogler, Leo Gschwind, Benno Röthlisberger, Andreas Huber, Isabel Filges, Peter Miny, Bianca Auschra, Attila Stetak, Philippe Demougin, Vanja Vukojevic, Iris-Tatjana Kolassa, Thomas Elbert, Dominique J-F de Quervain, Andreas Papassotiropoulos |
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Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2010-12-01
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Series: | PLoS ONE |
Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21179565/pdf/?tool=EBI |
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