A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv778771



Internal ID16072727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:70133454..70142028hg38UCSC Ensembl
Innerchr11:69979560..69988134hg19UCSC Ensembl
Innerchr11:69657208..69665782hg18UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg388575
hg198575
hg188575
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555336
Supporting Variants
Samples
Known GenesANO1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv778771
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer