Variant DetailsVariant: esv2719823Internal ID | 9954117 | Landmark | | Location Information | | Cytoband | 2p23.3 | Allele length | Assembly | Allele length | hg38 | 603 | hg19 | 603 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6689524, essv6898830, essv6832847, essv6787020, essv6919218, essv6789473, essv6896041, essv6671432, essv6892582, essv6739068, essv6902799, essv6829259, essv6707523, essv6946777, essv6836470, essv6785308, essv6914221, essv6751043 | Samples | SSM100, SSM036, SSM008, SSM083, SSM024, SSM013, SSM009, SSM041, SSM069, SSM003, SSM081, SSM082, SSM016, SSM005, SSM070, SSM099, SSM052, SSM098 | Known Genes | DTNB | 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) | esv2719823
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 18 | Observed Complex | 0 | Frequency | n/a |
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