A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555212



Internal ID15995935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:65535422..65540385hg38UCSC Ensembl
Innerchr11:65302893..65307856hg19UCSC Ensembl
Innerchr11:65059469..65064432hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg384964
hg194964
hg184964
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv777178, nssv777176, nssv777179, nssv777177
Samples
Known GenesLTBP3, SCYL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555212
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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