A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174618



Internal ID15533552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:36086947..36977835hg38UCSC Ensembl
Innerchr11:36108497..36999385hg19UCSC Ensembl
Innerchr11:36065073..36955961hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38890889
hg19890889
hg18890889
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554003
Supporting Variants
SamplesNINDS_178
Known GenesC11orf74, COMMD9, LDLRAD3, PRR5L, RAG1, RAG2, TRAF6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174618
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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