A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758254



Internal ID9980331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4886663..5114101hg38UCSC Ensembl
Innerchr11:4907893..5135331hg19UCSC Ensembl
Innerchr11:4864469..5091907hg18UCSC Ensembl
Innerchr11:4864469..5091907hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38227439
hg19227439
hg18227439
hg17227439
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759799
Supporting Variantsessv316, essv21853
SamplesNA11839, NA18971
Known GenesMMP26, OR51A2, OR51A4, OR51A7, OR51G1, OR51G2, OR51L1, OR52E2, OR52J3
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)esv2758254
Frequency
Sample Size270
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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