A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1175079



Internal ID15534396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:17372097..17396930hg38UCSC Ensembl
Innerchr11:17393644..17418477hg19UCSC Ensembl
Innerchr11:17350220..17375053hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3824834
hg1924834
hg1824834
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553583
Supporting Variants
SamplesNINDS_66
Known GenesABCC8, KCNJ11, NCR3LG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1175079
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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