A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556577



Internal ID15997300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:131680956..131681565hg38UCSC Ensembl
Innerchr11:131550850..131551459hg19UCSC Ensembl
Innerchr11:131056060..131056669hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38610
hg19610
hg18610
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv785114, nssv785116, nssv785113, nssv785115
Samples
Known GenesNTM
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556577
Frequency
Sample Size17421
Observed Gain3
Observed Loss1
Observed Complex0
Frequencyn/a


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