A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1418698



Internal ID15582482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5763465..5788132hg38UCSC Ensembl
Innerchr11:5784695..5809362hg19UCSC Ensembl
Innerchr11:5741271..5765938hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3824668
hg1924668
hg1824668
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv819430
Supporting Variants
SamplesAK1
Known GenesOR52N1, OR52N5
MethodOligo aCGH
AnalysisThe array was scanned with Agilent DNA microarray scanner at 2 micron resolution. The resulting image was extracted by Agilent's Feature Extraction software. The log2 ratios were analyzed using NEXUS software. Each aberration call was manually checked to confirm the accuracy of the calls.
PlatformGSE19651
Comments
ReferenceKim_et_al_2009
Pubmed ID19587683
Accession Number(s)nssv1418698
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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