Variant DetailsVariant: esv2715183![](http://dgv.tcag.ca/gb2/gbrowse_img/dgv2_hg38/?name=chr16:89634416..89635789;width=800;overview=1) Internal ID | 9949469 | Landmark | | Location Information | | Cytoband | 16q24.3 | Allele length | Assembly | Allele length | hg38 | 1374 | hg19 | 1374 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6772699, essv6835469, essv6792504, essv6863108, essv6953902, essv6920856, essv6888496, essv6905487, essv6706757, essv6728897, essv6966787, essv6867912, essv6732764, essv6788408, essv6665680, essv6913223, essv6796674, essv6721303, essv6949735, essv6936845, essv6674165, essv6971481, essv6941008, essv6688789, essv6685593, essv6945646, essv6820379 | Samples | SSM071, SSM027, SSM024, SSM046, SSM065, SSM013, SSM088, SSM023, SSM028, SSM021, SSM047, SSM069, SSM029, SSM096, SSM089, SSM017, SSM035, SSM031, SSM044, SSM040, SSM082, SSM015, SSM078, SSM022, SSM070, SSM025, SSM034 | Known Genes | DPEP1 | 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) | esv2715183
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 27 | Observed Complex | 0 | Frequency | n/a |
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