Variant DetailsVariant: esv2717683Internal ID | 9951974 | Landmark | | Location Information | | Cytoband | 18q23 | Allele length | Assembly | Allele length | hg38 | 288 | hg19 | 288 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6909668, essv6812827, essv6807010, essv6868196, essv6960745, essv6717685, essv6674551, essv6666164, essv6852566, essv6863404, essv6905712, essv6873231, essv6941276 | Samples | SSM011, SSM013, SSM074, SSM088, SSM029, SSM026, SSM089, SSM031, SSM014, SSM086, SSM076, SSM022, SSM043 | Known Genes | CTDP1 | 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) | esv2717683
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 13 | Observed Complex | 0 | Frequency | n/a |
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