Variant DetailsVariant: esv3599210 | Internal ID | 6986258 | | Landmark | | | Location Information | | | Cytoband | 3q29 | | Allele length | | Assembly | Allele length | | hg38 | 1259 | | hg19 | 1259 |
| | Variant Type | CNV loss | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | essv11284042, essv11283988, essv11284044, essv11283973, essv11284000, essv11284060, essv11283983, essv11284083, essv11283984, essv11284090, essv11283987, essv11283976, essv11284067, essv11284053, essv11283972, essv11283965, essv11284008, essv11284030, essv11284089, essv11284073, essv11284013, essv11284007, essv11284020, essv11284041, essv11284029, essv11283977, essv11284096, essv11284004, essv11284070, essv11284040, essv11284025, essv11284079, essv11284043, essv11284076, essv11284078, essv11284066, essv11284095, essv11284010, essv11283966, essv11283967, essv11284021, essv11284005, essv11283978, essv11283999, essv11283992, essv11284063, essv11284019, essv11284054, essv11283975, essv11284032, essv11284061, essv11284072, essv11283989, essv11284027, essv11284023, essv11284097, essv11284077, essv11284092, essv11284098, essv11284006, essv11284048, essv11284016, essv11283964, essv11284081, essv11283980, essv11284033, essv11284036, essv11283982, essv11284071, essv11284087, essv11284086, essv11284012, essv11284088, essv11284064, essv11284057, essv11284056, essv11284084, essv11284002, essv11284038, essv11283997, essv11284026, essv11284085, essv11284091, essv11284045, essv11284031, essv11283995, essv11283994, essv11283993, essv11284075, essv11284068, essv11284009, essv11283996, essv11283969, essv11284022, essv11284047, essv11284082, essv11283991, essv11283979, essv11284069, essv11284034, essv11283970, essv11284024, essv11283981, essv11283974, essv11284093, essv11283985, essv11283998, essv11284074, essv11284080, essv11283971, essv11284011, essv11284017, essv11284001, essv11284052, essv11284015, essv11283986, essv11284046, essv11284050, essv11284028, essv11284039, essv11284094, essv11284049, essv11284014, essv11284059, essv11284035, essv11284062, essv11284065, essv11284018, essv11283968, essv11284055, essv11284037, essv11283990, essv11284058, essv11284051, essv11284003 | | Samples | HG03690, HG01986, HG03773, HG01441, NA21089, HG02385, NA19204, NA12814, HG01885, HG03753, HG02433, HG01280, HG03300, HG02852, HG00315, NA18917, HG00181, HG02323, NA20298, HG03190, HG01802, HG03139, HG01632, HG03577, HG02589, HG03944, NA18510, NA19379, HG03016, HG03452, HG03976, HG03905, HG00158, HG01134, HG04214, HG04183, HG03817, HG01455, HG02561, HG02490, NA21107, HG03693, NA20412, NA19725, HG02427, HG03267, NA19445, HG03583, HG03585, HG03114, NA18867, NA19027, HG03270, HG02977, HG02439, NA19908, NA19247, HG03685, HG01187, HG02345, HG02582, HG02236, HG03786, NA19043, NA19236, HG02731, NA19982, HG02144, NA18910, HG02968, HG02878, HG00692, NA20876, HG03021, HG02789, HG01102, HG03301, NA21124, HG03476, HG02577, NA19042, HG03713, HG03802, HG01707, HG01504, NA19031, HG03953, HG03024, HG01890, HG03354, HG04118, HG01956, HG03694, NA19436, NA19035, HG02813, HG03238, NA20801, HG02667, HG04227, NA20276, NA19712, HG02501, HG02010, HG02721, HG02837, NA20790, NA20527, HG03127, NA19310, NA19467, HG02464, HG03557, HG02814, HG03103, NA19143, HG00111, HG03733, HG01783, HG02392, NA21101, NA20758, HG03470, HG03401, HG01914, HG01883, NA19121, HG01807, NA19129, HG03072, HG02284, NA20827, NA20585, HG03118, NA19214 | | Known Genes | | | Method | Sequencing | | Analysis | | | Platform | Multiple platforms | | Comments | | | Reference | 1000_Genomes_Consortium_Phase_3 | | Pubmed ID | 21293372 | | Accession Number(s) | esv3599210
| | Frequency | | Sample Size | 2504 | | Observed Gain | 0 | | Observed Loss | 135 | | Observed Complex | 0 | | Frequency | n/a |
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