A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555180



Internal ID15995903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:63748280..63945767hg38UCSC Ensembl
Innerchr11:63515752..63713239hg19UCSC Ensembl
Innerchr11:63272328..63469815hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38197488
hg19197488
hg18197488
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv777143
Samples
Known GenesC11orf84, C11orf95, MARK2, NAA40, RCOR2, RTN3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555180
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer