A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv778386



Internal ID16072342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:66944707..66945634hg38UCSC Ensembl
Innerchr11:66712178..66713105hg19UCSC Ensembl
Innerchr11:66468754..66469681hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38928
hg19928
hg18928
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555230
Supporting Variants
Samples
Known GenesPC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv778386
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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