A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8792



Internal ID15500018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:11853289..11855203hg38UCSC Ensembl
Outerchr11:11874836..11876750hg19UCSC Ensembl
Outerchr11:11831412..11833326hg18UCSC Ensembl
Outerchr11:11831412..11833326hg17UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg381915
hg191915
hg181915
hg171915
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv19905, nssv22735, nssv19556, nssv20677, nssv22604, nssv18199, nssv19730, nssv18245, nssv20648, nssv19626, nssv19606, nssv19894, nssv22171, nssv25081, nssv19074, nssv23415, nssv18011, nssv19923, nssv18962, nssv20035, nssv20379, nssv20129, nssv22906, nssv20878, nssv17860, nssv22063
SamplesNA12802, NA18975, NA19173, NA10839, NA10847, NA18972, NA18517, NA19144, NA18860, NA07029, NA10863, NA12155, NA12740, NA07048, NA18537, NA18572, NA12872, NA18504, NA19221, NA18552, NA19132, NA11830, NA19240, NA18853, NA19007, NA18980
Known GenesUSP47
MethodOligo aCGH
AnalysisStatistical threshold = 5.0, minimum +/- log2 ratio = 0.25 and minimum number of probes = 2
PlatformAgilent-015686 Custom Human 244K CGH Microarray
Comments
ReferencePerry_et_al_2008
Pubmed ID18304495
Accession Number(s)nsv8792
Frequency
Sample Size31
Observed Gain25
Observed Loss1
Observed Complex0
Frequencyn/a


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