A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556061



Internal ID16343470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:99313871..99315949hg38UCSC Ensembl
Innerchr11:99184602..99186680hg19UCSC Ensembl
Innerchr11:98689812..98691890hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg382079
hg192079
hg182079
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2117n54
Supporting Variantsnssv781750, nssv781745, nssv781742, nssv781752, nssv781741, nssv781740, nssv781739, nssv781744, nssv781753, nssv781737, nssv781738, nssv781751, nssv781746, nssv781747, nssv781743, nssv781749, nssv781748
Samples
Known GenesCNTN5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556061
Frequency
Sample Size17421
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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