A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5099



Internal ID9626750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55549600..55744786hg38UCSC Ensembl
Innerchr11:55317076..55512262hg19UCSC Ensembl
Innerchr11:55073652..55268838hg18UCSC Ensembl
Innerchr11:55073652..55268838hg17UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38195187
hg19195187
hg18195187
hg17195187
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758271
Supporting Variants
SamplesNA18577
Known GenesOR4C11, OR4C15, OR4C16, OR4C6, OR4P4, OR4S2
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)essv5099
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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