A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv785107



Internal ID15732377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:130576128..131154874hg38UCSC Ensembl
Innerchr11:130446023..131024769hg19UCSC Ensembl
Innerchr11:129951233..130529979hg18UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38578747
hg19578747
hg18578747
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556572
Supporting Variants
Samples
Known GenesC11orf44, MIR8052, SNX19
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv785107
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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