A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758289



Internal ID9633748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:131562907..131879091hg38UCSC Ensembl
Innerchr11:131432801..131748985hg19UCSC Ensembl
Innerchr11:130938011..131254195hg18UCSC Ensembl
Innerchr11:130938011..131254195hg17UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38316185
hg19316185
hg18316185
hg17316185
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759873
Supporting Variantsessv12271, essv11543, essv10363, essv16492, essv8158, essv19402, essv9660, essv21811, essv12379, essv16887, essv14629, essv4274, essv23558, essv9168, essv17306, essv15741
SamplesNA19222, NA18603, NA19131, NA06993, NA19238, NA19128, NA19210, NA19205, NA11839, NA11840, NA18856, NA19101, NA19206, NA18913, NA19173, NA19093
Known GenesNTM
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)esv2758289
Frequency
Sample Size270
Observed Gain16
Observed Loss0
Observed Complex0
Frequencyn/a


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