Non-Invasive Prenatal Testing (NIPT) for common microdeletions (Pilot)
Pilot - Not Accredited
Common microdeletion syndromes including: Prader Willi syndrome Angelman syndrome Williams syndrome Di-George syndrome
PURPOSE OF PROGRAMME:
Non-invasive prenatal testing (NIPT) for common microdeletions (pilot)
MATERIAL PROVIDED: Plasma
DISTRIBUTIONS PER YEAR: 1
SAMPLES PER DISTRIBUTION: 2-3
FREQUENCY OF DISTRIBUTION: 1
PROGRAMME OF ANALYSIS:
Detection of common microdeletion syndromes.
Details of the performance criteria for this programme can be obtained from UK NEQAS Genomics (GenQA) directly.
Telephone: +44 (0) 131 2426898
From 1st January 2018, Cytogenomics External Quality Assessment Service (CEQAS) and UK National External Quality Assessment Service (UK NEQAS) for Molecular Genetics merged to become Genomics Quality Assessment (GenQA). Please click here for an overview of GenQA