A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11189



Internal ID9608324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55692211..55854408hg38UCSC Ensembl
Innerchr11:55459687..55621884hg19UCSC Ensembl
Innerchr11:55216263..55378460hg18UCSC Ensembl
Innerchr11:55216263..55378460hg17UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38162198
hg19162198
hg18162198
hg17162198
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758271
Supporting Variants
SamplesNA19211
Known GenesOR5D13, OR5D14, OR5D16, OR5D18, OR5L1, OR5L2
MethodBAC aCGH
AnalysisArray images were acquired using an Agilent laser scanner (Agilent Technologies, UK). Fluorescence intensities and log2 ratio values were extracted using Bluefuse software (Bluegnome Ltd).
PlatformAgilent
Comments
ReferenceRedon_et_al_2006
Pubmed ID17122850
Accession Number(s)essv11189
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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