Variant DetailsVariant: esv2716691Internal ID | 9950979 | Landmark | | Location Information | | Cytoband | 18p11.31 | Allele length | Assembly | Allele length | hg38 | 1200 | hg19 | 1200 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6772850, essv6766194, essv6713675, essv6820549, essv6960568, essv6852394, essv6863266, essv6828446, essv6674375, essv6721435, essv6665970, essv6868081, essv6804034, essv6858363, essv6921019, essv6967035 | Samples | SSM027, SSM065, SSM087, SSM073, SSM042, SSM088, SSM029, SSM026, SSM089, SSM017, SSM031, SSM044, SSM086, SSM078, SSM080, SSM063 | Known Genes | DLGAP1 | 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) | esv2716691
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 16 | Observed Complex | 0 | Frequency | n/a |
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