Variant DetailsVariant: esv2748367Internal ID | 9982651 | Landmark | | Location Information | | Cytoband | 13q34 | Allele length | Assembly | Allele length | hg38 | 507 | hg19 | 507 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6691807, essv6936413, essv6966196, essv6959690, essv6851593, essv6732363, essv6977676, essv6842692, essv6835099, essv6728559, essv6924578, essv6713213, essv6973095, essv6920457 | Samples | SSM036, SSM027, SSM046, SSM042, SSM084, SSM021, SSM047, SSM018, SSM029, SSM026, SSM017, SSM086, SSM082, SSM004 | Known Genes | TMEM255B | 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) | esv2748367
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 14 | Observed Complex | 0 | Frequency | n/a |
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