Variant DetailsVariant: esv2717554 Internal ID | 9951845 | Landmark | | Location Information | | Cytoband | 18q23 | Allele length | Assembly | Allele length | hg38 | 716 | hg19 | 716 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6913480, essv6741768, essv6710202, essv6852544, essv6699306, essv6905693, essv6882928, essv6780317, essv6792750, essv6916923, essv6937101, essv6877308, essv6971733, essv6801141, essv6717671, essv6784464, essv6921115, essv6843341, essv6796926, essv6895407, essv6863389, essv6807000, essv6678675, essv6960719, essv6954156, essv6824471, essv6725341, essv6812865, essv6928648, essv6840542, essv6880092, essv6832118, essv6871341, essv6674527 | Samples | SSM071, SSM045, SSM079, SSM038, SSM013, SSM009, SSM093, SSM074, SSM088, SSM041, SSM028, SSM092, SSM084, SSM090, SSM021, SSM026, SSM017, SSM019, SSM094, SSM032, SSM031, SSM067, SSM086, SSM068, SSM081, SSM072, SSM015, SSM016, SSM010, SSM070, SSM025, SSM043, SSM052, 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) | esv2717554
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 34 | Observed Complex | 0 | Frequency | n/a |
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