A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174658



Internal ID15508972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:66700998..66866926hg38UCSC Ensembl
Innerchr11:66468469..66634397hg19UCSC Ensembl
Innerchr11:66225045..66390973hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38165929
hg19165929
hg18165929
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555225
Supporting Variants
Samples1782681216_A
Known GenesC11orf80, LRFN4, PC, RCE1, SPTBN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174658
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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