Variant DetailsVariant: esv2718880Internal ID | 9953172 | Landmark | | Location Information | | Cytoband | 19q13.42 | Allele length | Assembly | Allele length | hg38 | 490 | hg19 | 490 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6946194, essv6913733, essv6843604, essv6733234, essv6921434, essv6725561, essv6820942, essv6917190, essv6810182, essv6797172, essv6666546 | Samples | SSM071, SSM075, SSM045, SSM023, SSM084, SSM047, SSM029, SSM017, SSM015, SSM078, SSM016 | Known Genes | | 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) | esv2718880
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 11 | Observed Complex | 0 | Frequency | n/a |
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