A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1969n54



Internal ID18994145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65568234..65663889hg38UCSC Ensembl
chr11:65335705..65431360hg19UCSC Ensembl
chr11:65092281..65187936hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3895656
hg1995656
hg1895656
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv555213, nsv555214
Samples
Known GenesEHBP1L1, FAM89B, KCNK7, MAP3K11, MIR4489, MIR4690, PCNXL3, RELA, SIPA1, SSSCA1, SSSCA1-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1969n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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