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Letter
Nature Genetics 38, 75–81 (1 January 2006) | doi:10.1038/ng1697
A high-resolution survey of deletion polymorphism in the human genome
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Abstract
Recent work has shown that copy number polymorphism is an important class of genetic variation in human genomes. Here we report a new method that uses SNP genotype data from parent-offspring trios to identify polymorphic deletions.
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