Provides results of comparative genomic hybridization (CGH) analyses on more than 900 solid tumors of various types. MCG CNV Database offers copy number variant (CNV) and loss of heterozygosity (LOH) detected through microarray analyses in healthy Japanese population. This resource can be an assistance to estimate a pathogenicity of CNV or LOH detected in subjects having possible involvement of cryptic genomic aberrations behind their pathogenesis.
Department of Molecular Cytogenetics, Medical Research Institute and School of Biomedical Science, Tokyo, Japan; Center of Excellence Program for Frontier Research on Molecular Destruction and Reconstitution of Tooth and Bone, Tokyo Medical and Dental University, Tokyo, Japan; Core Research for Evolutional Science and Technology of Japan Science and Technology Corporation, Saitama, Japan
MCG CNV Database funding source(s)
Supported by Grants-in-Aid for Scientific Research on Priority Areas (C) and a Center of Excellence Program for Research on Molecular Destruction and Reconstruction of Tooth and Bone from the Ministry of Education, Culture, Sports, Science and Technology, Japan; and a Grant-in-Aid from Core Research for Evolutional Science and Technology of the Japan Science and Technology Corporation.