Variant DetailsVariant: esv2732748 Internal ID | 9967069 | Landmark | | Location Information | | Cytoband | 6q23.3 | Allele length | Assembly | Allele length | hg38 | 1139 | hg19 | 1139 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6705122, essv6711926, essv6676671, essv6822529, essv6767618, essv6841346, essv6694255, essv6934831, essv6961595, essv6865705, essv6684079, essv6939113, essv6770912, essv6907688, essv6860984, essv6943536, essv6774668, essv6811405, essv6918925, essv6855371, essv6761764, essv6723316, essv6915142, essv6790600, essv6719541, essv6715623, essv6969463, essv6679587, essv6881508, essv6849281, essv6802646, essv6896844, essv6962095, essv6875811, essv6680481, essv6845038, essv6805523, essv6887087, essv6884312, essv6794755, essv6708521, essv6903804, essv6808516, essv6830263, essv6701187, essv6671251, essv6697997, essv6798961, essv6687333, essv6727213, essv6833867, essv6786490, essv6888699, essv6826765, essv6729642, essv6869845, essv6930539, essv6923159, essv6911438, essv6957169, essv6926897, essv6782303, essv6899782, essv6893623, essv6929518, essv6878694, essv6872845, essv6837523, essv6778291, essv6730967, essv6826506, essv6796421, essv6951998, essv6814414 | Samples | SSM100, SSM008, SSM083, SSM071, SSM075, SSM045, SSM046, SSM064, SSM079, SSM065, SSM087, SSM038, SSM039, SSM013, SSM009, SSM073, SSM093, SSM074, SSM042, SSM088, SSM041, SSM023, SSM028, SSM092, SSM084, SSM090, SSM021, SSM047, SSM018, SSM069, SSM096, SSM026, SSM089, SSM017, SSM019, SSM035, SSM094, SSM032, SSM003, SSM031, SSM067, SSM044, SSM001, SSM014, SSM086, SSM033, SSM066, SSM085, SSM068, SSM081, SSM040, SSM072, SSM082, SSM020, SSM007, SSM015, SSM016, SSM005, SSM080, SSM037, SSM077, SSM076, SSM022, SSM010, SSM091, SSM070, SSM095, SSM025, SSM034, SSM004, SSM099, SSM043, SSM098, SSM012 | Known Genes | BCLAF1 | 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) | esv2732748
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 74 | Observed Complex | 0 | Frequency | n/a |
|
|