Variant DetailsVariant: esv2723123 | Internal ID | 10306759 | | Landmark | | | Location Information | | | Cytoband | 21p11.2 | | Allele length | | Assembly | Allele length | | hg38 | 3912 | | hg19 | 3912 |
| | Variant Type | CNV deletion | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | essv6707173, essv6888912, essv6836046, essv6703726, essv6836047, essv6733380, essv6682733, essv6747694, essv6961306, essv6921599, essv6950409, essv6675048, essv6807280, essv6928947, essv6836050, essv6859028, essv6843763, essv6972144, essv6917298, essv6909934, essv6810259, essv6859027, essv6843044, essv6967736, essv6949152, essv6692636, essv6902411, essv6901515, essv6721867, essv6874613, essv6885898, essv6824840, essv6733378, essv6846877, essv6863815, essv6821056, essv6925566, essv6797315, essv6868618, essv6686066, essv6853052, essv6729493, essv6933168, essv6696893, essv6675051, essv6721868, essv6937534, essv6972152, essv6902410, essv6725716, essv6721869, essv6961309, essv6804324, essv6689167, essv6902412, essv6675052, essv6696889, essv6917297, essv6901518, essv6813084, essv6875797, essv6906002, essv6773325, essv6941641, essv6902413, essv6895745, essv6883177, essv6692635, essv6949118, essv6868614, essv6895742, essv6714111, essv6946344, essv6950410, essv6898517, essv6784844, essv6789005, essv6885899, essv6797314, essv6747696, essv6804326, essv6816471, essv6797316, essv6913872, essv6913871, essv6933174, essv6892209, essv6780716, essv6871630, essv6832455, essv6954558, essv6895744, essv6784847, essv6972149, essv6843764, essv6933175, essv6967738, essv6776806, essv6846874, essv6954557, essv6692629, essv6933172, essv6780719, essv6915952, essv6880339, essv6885893, essv6863817, essv6682735, essv6793150, essv6915963, essv6807283, essv6824836, essv6718038, essv6925568, essv6789004, essv6710485, essv6950405, essv6828884, essv6793152, essv6853053, essv6853055, essv6769415, essv6810261, essv6707171, essv6801509, essv6721861, essv6967746, essv6801504, essv6921600, essv6898519, essv6696888, essv6941642 | | Samples | SSM100, SSM036, SSM071, SSM027, SSM024, SSM075, SSM045, SSM046, SSM011, SSM064, SSM079, SSM065, SSM087, SSM097, SSM039, SSM013, SSM073, SSM093, SSM074, SSM042, SSM088, SSM002, SSM041, SSM023, SSM028, SSM084, SSM090, SSM021, SSM047, SSM018, SSM069, SSM096, SSM026, SSM089, SSM017, SSM019, SSM035, SSM094, SSM003, SSM031, SSM067, SSM044, SSM014, SSM086, SSM033, SSM066, SSM085, SSM068, SSM081, SSM040, SSM072, SSM082, SSM020, SSM015, SSM078, SSM016, SSM080, SSM037, SSM077, SSM076, SSM022, SSM010, SSM091, SSM055, SSM070, SSM095, SSM025, SSM034, SSM099, SSM043, SSM098, SSM012 | | Known Genes | | | Method | Sequencing | | Analysis | Breakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads | | Platform | Illumina HiSeq 2000 | | Comments | | | Reference | Wong_et_al_2012b | | Pubmed ID | 23290073 | | Accession Number(s) | esv2723123
| | Frequency | | Sample Size | 96 | | Observed Gain | 0 | | Observed Loss | 72 | | Observed Complex | 0 | | Frequency | n/a |
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