homozygosity carrier analysis (array)

This test is available for the following conditions:

  • Conditions > Intellectual Disability > SNP array
  • Conditions > Multiple congenital anomalies (MCA) > SNP array
  • Conditions > Genome-wide analysis > SNP array

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





€ 750

Array

array analysis upon request (please specify in clinical information )

Turnaround time
5 weeks
Performing laboratory
Radboudumc
€ 750

array analysis upon request (please specify in clinical information )




€ 750

array analysis upon request (please specify in clinical information )

This test is available for the following conditions:

  • Conditions > Intellectual Disability > SNP array
  • Conditions > Multiple congenital anomalies (MCA) > SNP array
  • Conditions > Genome-wide analysis > SNP array

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.
Remarks
If Turner syndrome is strongly suspected, you can consider ordering the following test: 

Turner syndrome (chromosome analysis)

Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA





€ 750
Array

intellectual disability (array)

Turnaround time
5 weeks
Performing laboratory
Radboudumc
€ 750

intellectual disability (array)




€ 750

intellectual disability (array)

This test is available for the following conditions:

  • Conditions > Intellectual Disability > SNP array
  • Conditions > Multiple congenital anomalies (MCA) > SNP array
  • Conditions > Genome-wide analysis > SNP array

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





€ 750
Array

intellectual disability and multipele congenital anomalies (array)

Turnaround time
5 weeks
Performing laboratory
Radboudumc
€ 750

intellectual disability and multipele congenital anomalies (array)




€ 750

intellectual disability and multipele congenital anomalies (array)

This test is available for the following conditions:

  • Conditions > Intellectual Disability > SNP array
  • Conditions > Multiple congenital anomalies (MCA) > SNP array
  • Conditions > Genome-wide analysis > SNP array

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





€ 750
Array

multiple congenital abnormalities (array)

Turnaround time
5 weeks
Performing laboratory
Radboudumc
€ 750

multiple congenital abnormalities (array)




€ 750

multiple congenital abnormalities (array)

This test is available for the following conditions:

  • Conditions > Intellectual Disability > SNP array
  • Conditions > Multiple congenital anomalies (MCA) > SNP array
  • Conditions > Genome-wide analysis > SNP array

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





€ 750