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

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

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_swepub_primary_oai_DiVA_org_uu_136642

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

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

Structural variations of DNA greater than 1 kilobase in size account for most bases that vary among human genomes, but are still relatively under-ascertained. Here we use tiling oligonucleotide microarrays, comprising 42 million probes, to generate a comprehensive map of 11,700 copy number variations (CNVs) greater than 443 base pairs, of which mos...

Alternative Titles

Full title

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

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_swepub_primary_oai_DiVA_org_uu_136642

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_swepub_primary_oai_DiVA_org_uu_136642

Other Identifiers

ISSN

0028-0836,1476-4687

E-ISSN

1476-4687

DOI

10.1038/nature08516