A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3503439



Internal ID18801720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:37917683..37954795hg38UCSC Ensembl
Innerchr11:37939233..37976345hg19UCSC Ensembl
Innerchr11:37895809..37932921hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3837113
hg1937113
hg1837113
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036207
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3503439
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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