Variant DetailsVariant: dgv531e201Internal ID | 20125418 | Landmark | | Location Information | | Cytoband | 19q13.42 | Allele length | Assembly | Allele length | hg19 | 1055 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | esv2718901, esv2718896, esv2718903, esv2718893 | Samples | SSM083, SSM071, SSM027, SSM075, SSM045, SSM011, SSM064, SSM079, SSM087, SSM038, SSM097, SSM039, SSM073, SSM074, SSM088, SSM023, SSM028, SSM084, SSM090, SSM018, SSM096, SSM026, SSM089, SSM094, SSM032, SSM031, SSM014, SSM086, SSM066, SSM006, SSM072, SSM007, SSM078, SSM005, SSM080, SSM076, SSM025, SSM034, SSM043, SSM098 | 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) | dgv531e201
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 40 | Observed Complex | 0 | Frequency | n/a |
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