A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174281



Internal ID15532609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1853174..1891496hg38UCSC Ensembl
Innerchr11:1874404..1912726hg19UCSC Ensembl
Innerchr11:1830980..1869302hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3838323
hg1938323
hg1838323
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553057
Supporting Variants
SamplesHGDP01339
Known GenesLSP1, MIR4298
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174281
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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