Variant DetailsVariant: esv2750393Internal ID | 9984677 | Landmark | | Location Information | | Cytoband | 16p13.3 | Allele length | Assembly | Allele length | hg38 | 395 | hg19 | 395 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv323e201 | Supporting Variants | essv6936653, essv6871086, essv6728747, essv6901757, essv6828178, essv6721145, essv6928311, essv6895069, essv6835316, essv6920710, essv6897984, essv6971330 | Samples | SSM046, SSM028, SSM090, SSM021, SSM017, SSM019, SSM044, SSM082, SSM080, SSM099, SSM098, SSM012 | Known Genes | MMP25 | 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) | esv2750393
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 12 | Observed Complex | 0 | Frequency | n/a |
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