A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552854



Internal ID16340263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:511805..619789hg38UCSC Ensembl
Innerchr11:511805..619789hg19UCSC Ensembl
Innerchr11:501805..609789hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38107985
hg19107985
hg18107985
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174586
Samples1780862487_A
Known GenesC11orf35, CDHR5, HRAS, IRF7, LOC143666, LRRC56, MIR210, MIR210HG, PHRF1, RASSF7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552854
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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