A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9798826



Internal ID18681039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107777826..107801319hg38UCSC Ensembl
Innerchr11:107648552..107672045hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3823494
hg1923494
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3580094
Supporting Variants
Samples401611CD
Known GenesSLC35F2
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=24
ReferenceUddin_et_al_2014
Pubmed ID25503493
Accession Number(s)essv9798826
Frequency
Sample Size873
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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