Variant DetailsVariant: esv3616406Internal ID | 6656603 | Landmark | | Location Information | | Cytoband | 8p22 | Allele length | Assembly | Allele length | hg38 | 13128 | hg19 | 13128 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv13118032, essv13117993, essv13117963, essv13117957, essv13117946, essv13118016, essv13117996, essv13117938, essv13117976, essv13117961, essv13118014, essv13117953, essv13117929, essv13118028, essv13117935, essv13117920, essv13117958, essv13118035, essv13118026, essv13117988, essv13118036, essv13118039, essv13117932, essv13118042, essv13117980, essv13117970, essv13118021, essv13117962, essv13117968, essv13118010, essv13117998, essv13117973, essv13117940, essv13117984, essv13117928, essv13118025, essv13117950, essv13117919, essv13117967, essv13117949, essv13117991, essv13118044, essv13118023, essv13117952, essv13118000, essv13118027, essv13118038, essv13117917, essv13117964, essv13118022, essv13117942, essv13118024, essv13117977, essv13118018, essv13118009, essv13117947, essv13117987, essv13117943, essv13117960, essv13118005, essv13117921, essv13117959, essv13117979, essv13117955, essv13118001, essv13118034, essv13118011, essv13117954, essv13117916, essv13118033, essv13118012, essv13118019, essv13117934, essv13117997, essv13118007, essv13117941, essv13118008, essv13117948, essv13117989, essv13117915, essv13117995, essv13118020, essv13117990, essv13117918, essv13117927, essv13117972, essv13117930, essv13118029, essv13117924, essv13117944, essv13117936, essv13117925, essv13117965, essv13118043, essv13117923, essv13117956, essv13118013, essv13118002, essv13117971, essv13117969, essv13117937, essv13117992, essv13118003, essv13117966, essv13118006, essv13117945, essv13117931, essv13118041, essv13117985, essv13117939, essv13117926, essv13118017, essv13117951, essv13117922, essv13117986, essv13117975, essv13117999, essv13118040, essv13117982, essv13117914, essv13118037, essv13118004, essv13117983, essv13117978, essv13118031, essv13117981, essv13117933, essv13117994, essv13117974, essv13118015, essv13118030 | Samples | HG00096, NA20761, HG02072, HG01965, HG01624, HG01773, NA18565, HG02026, HG02035, HG01815, HG03767, HG02661, HG03015, HG01970, HG00315, HG00151, HG04076, HG01802, HG00737, NA18633, HG02023, HG01809, NA18962, NA12399, NA20806, HG04059, HG00663, HG00717, NA19076, HG02153, HG00589, HG02016, HG03913, HG02085, HG02374, HG04131, HG03762, HG03594, HG02395, NA12156, HG01046, HG01308, HG02164, HG02402, HG01784, HG01139, HG00154, HG00560, HG01841, NA19082, HG02070, HG03718, HG02513, NA19086, HG01864, HG01088, HG03711, HG00584, NA18637, NA18579, HG01345, NA18534, HG01852, NA12234, NA19064, NA18566, HG01392, HG01619, NA20901, NA19655, NA21112, NA11840, HG01504, HG02121, HG01241, HG01791, NA18532, HG01130, HG00525, NA19059, HG04063, HG02725, HG02031, NA20828, HG01865, HG00864, HG01811, HG03934, NA18608, NA20799, HG00611, HG03598, HG00254, HG01597, HG04026, NA12775, HG02355, HG02064, HG00734, HG01874, HG00638, HG02391, HG01798, NA19741, NA07037, NA21094, HG00620, HG01861, HG02401, HG01846, HG00267, NA12830, HG04209, HG01600, HG00112, HG03925, HG02681, NA18983, HG01914, HG01479, NA20503, HG00472, NA18957, NA18624, NA18623, HG01869, NA19065, HG01061, HG02060, NA18620, HG00593 | Known Genes | TUSC3 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3616406
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 131 | Observed Complex | 0 | Frequency | n/a |
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