A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552776



Internal ID15993499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:366710..432436hg38UCSC Ensembl
Innerchr11:366710..432436hg19UCSC Ensembl
Innerchr11:356710..422436hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3865727
hg1965727
hg1865727
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1175075
Samples1780862300_A
Known GenesANO9, B4GALNT4, PKP3, SIGIRR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552776
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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