A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758282



Internal ID9980359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:90875033..91186887hg38UCSC Ensembl
Innerchr11:90608201..90920055hg19UCSC Ensembl
Innerchr11:90247849..90559703hg18UCSC Ensembl
Innerchr11:90247849..90559703hg17UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38311855
hg19311855
hg18311855
hg17311855
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759850
Supporting Variantsessv22118, essv15364, essv23667, essv12550, essv18386, essv13420, essv9440, essv2974, essv1494, essv10483, essv23888, essv18828, essv10228, essv24069, essv17227, essv15068, essv12470, essv1127, essv14416, essv19603, essv2630, essv1782, essv10786, essv17033, essv5753, essv15212, essv2296, essv23782, essv13664, essv10111, essv23339, essv10883, essv9901, essv8829, essv1833, essv22182, essv3536, essv13804, essv11157, essv8464, essv3177, essv24984, essv19938, essv5256, essv19658, essv22772, essv17668, essv22668, essv9055, essv2486, essv10642, essv11940, essv8155, essv19000, essv21130, essv248, essv23559, essv7300, essv17169, essv17100, essv10429, essv12338, essv11865, essv23981, essv18116, essv23016, essv9993, essv10516, essv13163, essv23492, essv17445, essv13600, essv12847, essv1223, essv5470, essv11669, essv9204, essv19567, essv4446, essv8354, essv1422, essv21344, essv8650, essv20960, essv146, essv21284, essv11816, essv20393, essv10285, essv2183, essv17305, essv9372, essv23608, essv15392, essv23225, essv21819, essv8758, essv18429, essv1032, essv19985, essv15795, essv14190, essv19419, essv16136, essv22332, essv20663, essv15515, essv12255, essv13544, essv10950, essv6226, essv1971, essv21219, essv3998, essv16085, essv14608, essv8288, essv12418, essv13893, essv22525, essv1342, essv17809, essv11752, essv20130, essv7835, essv20593, essv22085, essv23440, essv17543, essv5179, essv9123, essv5935, essv11456, essv9621, essv9729, essv11027, essv15545, essv22949, essv300, essv5140, essv14265, essv21440, essv16196, essv4581, essv22533, essv20336, essv3309, essv9766, essv15860, essv407, essv15678, essv13027, essv24235, essv12629, essv16861, essv14896, essv13057, essv24591, essv7717, essv18637, essv6633, essv24932, essv22398, essv4637, essv16729, essv20996, essv3217, essv18202, essv14716, essv22900, essv14573, essv8234, essv6970, essv1186, essv8961, essv21394, essv24368, essv16409, essv16776, essv24801
SamplesNA18502, NA19141, NA12717, NA19222, NA11830, NA19203, NA18621, NA18862, NA18592, NA18508, NA12814, NA18524, NA18980, NA18855, NA12236, NA19145, NA18999, NA19092, NA12751, NA07029, NA12801, NA18504, NA18959, NA10857, NA19098, NA18633, NA12750, NA12155, NA07357, NA12813, NA18967, NA19127, NA19192, NA19171, NA19005, NA18944, NA18550, NA12812, NA19201, NA18995, NA10854, NA19119, NA18860, NA18558, NA19131, NA18960, NA11992, NA07048, NA18582, NA12762, NA19138, NA18964, NA06993, NA19130, NA18611, NA12005, NA18970, NA07019, NA19137, NA19238, NA12044, NA19207, NA19172, NA19128, NA18966, NA12815, NA19159, NA10855, NA19239, NA19209, NA10839, NA19200, NA11993, NA19007, NA11831, NA18951, NA12760, NA12752, NA19120, NA19194, NA10863, NA10831, NA19152, NA12878, NA19161, NA18859, NA18515, NA19205, NA18516, NA18871, NA19103, NA18976, NA18948, NA18503, NA11839, NA18981, NA12234, NA19208, NA19221, NA19202, NA19142, NA11840, NA10830, NA18856, NA12249, NA18912, NA12892, NA19154, NA18857, NA18853, NA12264, NA19099, NA12707, NA19101, NA07345, NA06985, NA18523, NA19160, NA19132, NA10856, NA18858, NA18593, NA19012, NA18974, NA12043, NA19094, NA18978, NA18632, NA11882, NA19206, NA06991, NA12716, NA11881, NA12864, NA18863, NA18564, NA12057, NA10859, NA19140, NA18913, NA19240, NA19100, NA19144, NA07348, NA12763, NA18594, NA19143, NA18501, NA12740, NA06994, NA18971, NA19223, NA19211, NA19093, NA10860, NA18636, NA18521, NA18500, NA18506, NA19102, NA12875, NA18854, NA19116, NA18972, NA18872, NA18552, NA18852, NA07056, NA18505, NA19129, NA18968, NA18624, NA19139, NA12006, NA18522, NA12154, NA07034, NA19153, NA18965, NA18997
Known GenesDISC1FP1
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)esv2758282
Frequency
Sample Size270
Observed Gain180
Observed Loss0
Observed Complex0
Frequencyn/a


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