Variant DetailsVariant: esv2715190Internal ID | 9949476 | Landmark | | Location Information | | Cytoband | 16q24.3 | Allele length | Assembly | Allele length | hg38 | 903 | hg19 | 903 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6831906, essv6843091, essv6815980, essv6810844, essv6691310, essv6971482, essv6728899, essv6710004, essv6901080, essv6743044, essv6714610, essv6928456, essv6960312, essv6665681, essv6763755, essv6895199, essv6824244, essv6696207, essv6792505, essv6852160, essv6699160 | Samples | SSM100, SSM046, SSM079, SSM038, SSM009, SSM041, SSM028, SSM084, SSM029, SSM062, SSM026, SSM019, SSM086, SSM006, SSM081, SSM007, SSM005, SSM037, SSM077, SSM070, SSM098 | Known Genes | CHMP1A | 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) | esv2715190
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 21 | Observed Complex | 0 | Frequency | n/a |
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