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Keywords: 631/208/1405; 631/208/1516; 631/208/514/2254; 692/700/139/1512; Abortion, Spontaneous - genetics; Biomedicine; Chromosome Disorders - diagnosis; Chromosome Disorders - genetics; Chromosome Disorders - pathology; Cytogenetics - methods; DNA Copy Number Variations - genetics; Female; Genome, Human - genetics; High-Throughput Nucleotide Sequencing; Human Genetics; Humans; Laboratory Medicine; Male; Microarray Analysis; original-research-article; Prenatal Diagnosis; Stillbirth - genetics; next-generation sequencing; molecular karyotyping; pathogenic copy-number variants