Variant DetailsVariant: esv2718493 Internal ID | 9952784 | Landmark | | Location Information | | Cytoband | 19q13.12 | Allele length | Assembly | Allele length | hg38 | 12599 | hg19 | 12598 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6925366, essv6971944, essv6816328, essv6741902, essv6880232, essv6913689, essv6905846, essv6917128, essv6883066, essv6941442, essv6824667, essv6753310, essv6841831, essv6788829, essv6961015, essv6725512, essv6753308, essv6807157, essv6921366, essv6797129, essv6747575, essv6839666 | Samples | SSM083, SSM071, SSM045, SSM079, SSM013, SSM093, SSM074, SSM057, SSM028, SSM018, SSM069, SSM026, SSM017, SSM094, SSM015, SSM016, SSM077, SSM022, SSM010, SSM055, SSM052 | Known Genes | FFAR1, FFAR3 | 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) | esv2718493
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 21 | Observed Complex | 0 | Frequency | n/a |
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