A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556109



Internal ID16343518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:99722154..99760844hg38UCSC Ensembl
Innerchr11:99592885..99631575hg19UCSC Ensembl
Innerchr11:99098095..99136785hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3838691
hg1938691
hg1838691
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2129n54
Supporting Variantsnssv781981
Samples
Known GenesCNTN5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556109
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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