A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7020262



Internal ID10350353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107467227..107476508hg38UCSC Ensembl
Innerchr11:107337953..107347234hg19UCSC Ensembl
Innerchr11:106843163..106852444hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg389282
hg199282
hg189282
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2760168
Supporting Variants
SamplesRW_0637
Known Genes
MethodMerging
AnalysisTwo different algorithms (PennCNV and Birdseye) were applied to detect CNVs. Only congruent CNV events regarding direction of effect that were detected by both algorithms were merged using the outer borders of the event in a first step. In a second step only CNVs that were detected in at least two individuals were merged into a CNVR.
PlatformMerging
Comments
ReferenceVogler_et_al_2010
Pubmed ID21179565
Accession Number(s)essv7020262
Frequency
Sample Size1109
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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