A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176200



Internal ID15533680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:128903518..128934894hg38UCSC Ensembl
Innerchr11:128773413..128804789hg19UCSC Ensembl
Innerchr11:128278623..128309999hg18UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3831377
hg1931377
hg1831377
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556563
Supporting Variants
SamplesNINDS_200
Known GenesC11orf45, KCNJ5, TP53AIP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176200
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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