Variant DetailsVariant: esv2722942Internal ID | 9957242 | Landmark | | Location Information | | Cytoband | 20q13.33 | Allele length | Assembly | Allele length | hg38 | 286 | hg19 | 286 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv679e201 | Supporting Variants | essv6892028, essv6852712, essv6832209, essv6706964, essv6824572, essv6895486, essv6871404, essv6863507, essv6892029, essv6909737, essv6824573, essv6792863, essv6733101 | Samples | SSM079, SSM097, SSM088, SSM090, SSM047, SSM014, SSM086, SSM081, SSM040, SSM070, SSM098 | Known Genes | HELZ2 | 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) | esv2722942
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 11 | Observed Complex | 0 | Frequency | n/a |
|
|