NL
acute lymphoblastic leukemia (ALL, please send in DNA)
Turnaround time
4 weeks
Method
- Array; Deletion/duplication analysis with the ThermoFisher CytoScan HD array platform containing 2,696,550 copy number markers (of which 743,304 are SNP markers) distributed over the human genome. The genome wide practical resolution averages ~20 kb.
Please send isolated DNA.
Performing laboratory: Radboudumc
Authorized material(s): Bone marrow
carrier testing (CNV)
This test is available for the following conditions:
- Conditions > Genome-wide analysis > Healthy individual
Turnaround time
5 weeks
Method
- Array; Deletion/duplication analysis with the ThermoFisher CytoScan HD array platform containing 2,696,550 copy number markers (of which 743,304 are SNP markers) distributed over the human genome. The genome wide practical resolution averages ~20 kb.
- Deletion/duplication analysis with the ThermoFisher CytoScan XON array platform containing 6,85 million copy number markers (of which 300.000 are SNP markers) with an excellent exon coverage (both coding as non-coding exons). The genome wide practical resolution averages ~100 kb.
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA
chronic lymphoblastic leukemia (CLL, please send in EDTA blood or DNA)
Turnaround time
4 weeks
Method
- Array; Deletion/duplication analysis with the ThermoFisher CytoScan HD array platform containing 2,696,550 copy number markers (of which 743,304 are SNP markers) distributed over the human genome. The genome wide practical resolution averages ~20 kb.
please send in EDTA blood or DNA
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA
intellectual disability (CNV)
This test is available for the following conditions:
- Conditions > Intellectual Disability > CNV in WES / SNP-based array
- Conditions > Multiple congenital anomalies (MCA) > CNV in WES / SNP-based array
- Conditions > Genome-wide analysis > CNV in WES / SNP-based array
Turnaround time
5 weeks
Method
- Exome-wide CNV analysis in the exome data is a validated, good and efficient alternative that has a comparable diagnostic yield as genome-wide array analysis, but also offers the possibility to successively or simultaneously assess copy number variants (CNVs) and nucleotide variants (SNVs) in one test . The genome-wide practical resolution is on average 100-200 kb.
- Array; Deletion/duplication analysis with the ThermoFisher CytoScan HD array platform containing 2,696,550 copy number markers (of which 743,304 are SNP markers) distributed over the human genome. The genome wide practical resolution averages ~20 kb.
- Deletion/duplication analysis with the ThermoFisher CytoScan XON array platform containing 6,85 million copy number markers (of which 300.000 are SNP markers) with an excellent exon coverage (both coding as non-coding exons). The genome wide practical resolution averages ~100 kb.
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA
intellectual disability and multipele congenital anomalies (CNV)
This test is available for the following conditions:
- Conditions > Intellectual Disability > CNV in WES / SNP-based array
- Conditions > Multiple congenital anomalies (MCA) > CNV in WES / SNP-based array
- Conditions > Genome-wide analysis > CNV in WES / SNP-based array
Turnaround time
5 weeks
Method
- Exome-wide CNV analysis in the exome data is a validated, good and efficient alternative that has a comparable diagnostic yield as genome-wide array analysis, but also offers the possibility to successively or simultaneously assess copy number variants (CNVs) and nucleotide variants (SNVs) in one test . The genome-wide practical resolution is on average 100-200 kb.
- Array; Deletion/duplication analysis with the ThermoFisher CytoScan HD array platform containing 2,696,550 copy number markers (of which 743,304 are SNP markers) distributed over the human genome. The genome wide practical resolution averages ~20 kb.
- Deletion/duplication analysis with the ThermoFisher CytoScan XON array platform containing 6,85 million copy number markers (of which 300.000 are SNP markers) with an excellent exon coverage (both coding as non-coding exons). The genome wide practical resolution averages ~100 kb.
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA
multiple congenital abnormalities (CNV)
This test is available for the following conditions:
- Conditions > Intellectual Disability > CNV in WES / SNP-based array
- Conditions > Multiple congenital anomalies (MCA) > CNV in WES / SNP-based array
- Conditions > Genome-wide analysis > CNV in WES / SNP-based array
Turnaround time
5 weeks
Method
- Exome-wide CNV analysis in the exome data is a validated, good and efficient alternative that has a comparable diagnostic yield as genome-wide array analysis, but also offers the possibility to successively or simultaneously assess copy number variants (CNVs) and nucleotide variants (SNVs) in one test . The genome-wide practical resolution is on average 100-200 kb.
- Array; Deletion/duplication analysis with the ThermoFisher CytoScan HD array platform containing 2,696,550 copy number markers (of which 743,304 are SNP markers) distributed over the human genome. The genome wide practical resolution averages ~20 kb.
- Deletion/duplication analysis with the ThermoFisher CytoScan XON array platform containing 6,85 million copy number markers (of which 300.000 are SNP markers) with an excellent exon coverage (both coding as non-coding exons). The genome wide practical resolution averages ~100 kb.
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA
