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PMID: 16494531
DOI: 10.1371/journal.pbio.0040072

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In this knowledge base

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Origins and functional impact of copy number variation in the human genome.	2010	19812545
A second generation human haplotype map of over 3.1 million SNPs.	2007	17943122

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    paperKB 97c16d336ceac0eb2a02388a7f94abfe40896884
  