A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv770387



Internal ID16064343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:29157407..29199747hg38UCSC Ensembl
Innerchr11:29178954..29221294hg19UCSC Ensembl
Innerchr11:29135530..29177870hg18UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3842341
hg1942341
hg1842341
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553940
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv770387
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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