A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556055



Internal ID16343464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:99215777..99225748hg38UCSC Ensembl
Innerchr11:99086508..99096479hg19UCSC Ensembl
Innerchr11:98591718..98601689hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg389972
hg199972
hg189972
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv781727
Samples
Known GenesCNTN5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556055
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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