Rsrc
J-GLOBAL ID：201410055708755453
Research Resource code：NBDC01141
Update date：Jun. 17, 2013
MCG CNV Database
MCG CNV Database
Resource classification：
Data,Database
Tag (subject) (2)：
Genetic variation
, Health/Disease
Tag (data type) (1)：
Expression
Species (1)：
Homo sapiens (NCBI Taxonomy ID: 9606)
Overview：
This database is called MCG CNV and provides copy number variant (CNV) and loss of heterozygosity (LOH) data. These have been detected by microarray analyses using MCG arrays and SNP arrays. The incidence of CNV and LOH in healthy Japanese is available. This is essential to assess the pathogenicity of CNV or LOH, and to differentiate between "pathogenic" and "benign" CNV, which is useful in patients with pathology due to cryptic genomic aberrations.
Source：
NBDC
Record maintainer：
Integbio Database Catalog
Record license：
Creative Commons CC0 license
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