A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9799094



Internal ID18337961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:125589845..125596781hg38UCSC Ensembl
Innerchr11:125459740..125466676hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg386937
hg196937
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3579952
Supporting Variants
Samples401734PG
Known GenesSTT3A
MethodSNP array
AnalysisWe used four separate algorithms to detect CNVs; Affymetrix Chromosome Analysis Suite (ChAS), iPattern, Nexus and Partek. Our primary analysis was performed based on ChAS CNV calls, which were then supported using the remaining three algorithms to construct a confidence set of CNVs. For all algorithms, we have used 8 probes and >1kb as a base line cutoff for CNV detection.
PlatformAffymetrix CytoScan HD 2.7M array
CommentsNumber of probes=8
ReferenceUddin_et_al_2014
Pubmed ID25503493
Accession Number(s)essv9799094
Frequency
Sample Size873
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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