esv29944
- Organism: Homo sapiens
- Study:estd21 (Wheeler et al. 2008)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Yes
- Clinical Assertions: No
- Region Size:82,635
- Publication(s):Wheeler et al. 2008
Source: NCBI
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 2669 SVs from 106 studies. See in: genome view
Overlapping variant regions from other studies: 2676 SVs from 106 studies. See in: genome view
Overlapping variant regions from other studies: 936 SVs from 33 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv29944 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 55,600,678 | 55,683,312 |
| esv29944 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 55,368,154 | 55,450,788 |
| esv29944 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000011.8 | Chr11 | 55,124,730 | 55,207,364 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv84183 | copy number loss | WATSON | Oligo aCGH | Probe signal intensity | 23 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv84183 | Remapped | Perfect | NC_000011.10:g.(?_ 55600678)_(5568331 2_?)del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 55,600,678 | 55,683,312 |
| essv84183 | Remapped | Perfect | NC_000011.9:g.(?_5 5368154)_(55450788 _?)del | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 55,368,154 | 55,450,788 |
| essv84183 | Submitted genomic | NC_000011.8:g.(?_5 5124730)_(55207364 _?)del | NCBI36 (hg18) | NC_000011.8 | Chr11 | 55,124,730 | 55,207,364 |
Validation Information
| Variant Call ID | Experiment ID | Sample ID | Method | Analysis | Result |
|---|---|---|---|---|---|
| essv84183 | 2 | WATSON | Oligo aCGH | Probe signal intensity | Pass |
| essv84183 | 4 | WATSON | Oligo aCGH | Probe signal intensity | Pass |
| essv84183 | 3 | WATSON | Sequencing | Read depth | Pass |