Acquired Copy Number Alterations in Adult Acute Myeloid Leukemia Genomes
Demographics (2)
- Age at entry - Age at diagnosis (phv00076149.v1.p1)
- Sex - Gender of participant (phv00076146.v1.p1)
Disease Events (2)
- AFFECTION_STATUS - Affection Status (phv00076184.v1.p1)
- case_control - Case or control? (phv00076144.v1.p1)
Race and Ethnicity (1)
- Race - Subject's Race (phv00076150.v1.p1)
Other (42)
- %BM Blast @ diagnosis - What percentage of myeloblasts were present in the bone marrow at the time of diagnosis? (phv00076147.v1.p1)
- %PB Blast - What percentage of blasts were present in the peripheral blood at diagnosis? (phv00076151.v1.p1)
- Abnormal/Total Cells (clone 1) - # of abnormal cells in clone 1/total cells evaluated (if applicable) (phv00076156.v1.p1)
- Abnormal/Total Cells (Clone 2) - # of abnormal cells in clone 2/total cells evaluated (if applicable) (phv00076158.v1.p1)
- Abnormal/Total Cells (clone 3) - # of abnormal cells in clone 3/total cells evaluated (if applicable) (phv00076160.v1.p1)
- Abnormal/Total Cells (clone 4) - # of abnormal cells in clone 4/total cells evaluated (if applicable) (phv00076162.v1.p1)
- Abnormal/Total Cells (clone 5) - # of abnormal cells in clone 5/total cells evaluated (if applicable) (phv00076164.v1.p1)
- c-Kit - Does participant have a somatic mutation in c-KIT (Entrez GeneID: 3815)? (phv00076171.v1.p1)
- CEBPA - Does participant have a somatic mutation in CEBPA (Entrez GeneID: 1050)? (phv00076175.v1.p1)
- CONSENT - Consent group as determined by DAC (phv00076181.v1.p1)
- Cytogenetics Clone 1 - Cytogenetic abnormality found in clone 1 (if applicable) (phv00076155.v1.p1)
- Cytogenetics Clone 2 - Cytogenetic abnormality found in clone 2 (if applicable) (phv00076157.v1.p1)
- Cytogenetics Clone 4 - Cytogenetic abnormality found in clone 4 (if applicable) (phv00076161.v1.p1)
- Cytogenetics Clone 5 - Cytogenetic abnormality found in clone 5 (if applicable) (phv00076163.v1.p1)
- Cytogenetics Clone3 - Cytogenetic abnormality found in clone 3 (if applicable) (phv00076159.v1.p1)
- ETV6 - Does participant have a somatic mutation in ETV6 (Entrez GeneID: 2120)? (phv00076168.v1.p1)
- FAB - French-American-British (FAB) classification category for bone marrow biopsy and aspirate (phv00076145.v1.p1)
- FLT3 - D835 - Does participant have a somatic D835 mutation in FLT3 (Entrez GeneID: 2322)? (phv00076170.v1.p1)
- FLT3 - ITD - Does participant have a somatic internal tandem duplication (ITD) in FLT3 (Entrez GeneID: 2322)? (phv00076169.v1.p1)
- KRAS - Does participant have a somatic mutation in KRAS (Entrez GeneID: 3845)? (phv00076173.v1.p1)
- months of EFS (as of 10/28/08) - # of months of Event Free Survival (phv00076166.v1.p1)
- months of OS (as of 10/28/08) - # of months of Overall Survival (phv00076165.v1.p1)
- NPM1 - Does participant have a somatic mutation in NPM1 (Entrez GeneID: 4869)? (phv00076174.v1.p1)
- NRAS - Does participant have a somatic mutation in NRAS (Entrez GeneID: 4893)? (phv00076172.v1.p1)
- NUP98 fusion - Does participant have a NUP98 fusion (Entrez GeneID: 4928)? (phv00076167.v1.p1)
- p53 - Does participant have a somatic mutation in p53 (Entrez GeneID: 7157)? (phv00076177.v1.p1)
- Patient expired - Has patient expired? (phv00076154.v1.p1)
- PB WBC @ diagnosis - What was the peripheral blood White Blood Cell Count at diagnosis? (phv00076148.v1.p1)
- PTPN11 - Does participant have a somatic mutation in PTPN11 (Entrez GeneID: 5781)? (phv00076176.v1.p1)
- RUNX1 - Does participant have a somatic mutation in RUNX1 (Entrez GeneID: 861)? (phv00076178.v1.p1)
- SAMP_SOURCE - Source repository where samples originate (phv00076187.v1.p1)
- SAMPID - CEL file and txt file chip ID (phv00076186.v1.p1)
- SOURCE_SAMPID - Sample ID used in the Source Repository (phv00076189.v1.p1)
- SOURCE_SUBJID - Subject ID used in the Source Repository (phv00076183.v1.p1)
- SPI1 - Does participant have a somatic mutation in SPI1 (Entrez GeneID: 6688)? (phv00076179.v1.p1)
- SUBJ_SOURCE - Source repository where subjects originate (phv00076182.v1.p1)
- SUBJID - Deidentified Subject's ID/Unique Patient Name (UPN) (phv00076143.v1.p1)
- SUBJID - Deidentified Subject's ID/Unique Patient Name (UPN) (phv00076180.v1.p1)
- SUBJID - Deidentified Subject's ID/Unique Patient Name (UPN) (phv00076185.v1.p1)
- TISSUE - Tissue of origin from which sample was made (phv00076188.v1.p1)
- Transplant Type - Type(s) of transplant patient received, if any (phv00076153.v1.p1)
- Treatment Protocol - Treatment protocol given to patient (phv00076152.v1.p1)