DNA Copy Number VariationsGene DosageAdenomatoid TumorGenetic VariationOligonucleotide Array Sequence AnalysisComparative Genomic HybridizationGenome, HumanPolymorphism, Single NucleotideBase SequencePolymerase Chain ReactionMolecular Sequence DataGenotypeGene DuplicationGenomicsSequence Analysis, DNAChromosome AberrationsChromosome MappingGenome-Wide Association StudyGenetic Predisposition to DiseaseNucleic Acid HybridizationGenomeSegmental Duplications, GenomicChromosomes, Artificial, BacterialChromosomes, HumanGene AmplificationDNA, NeoplasmAlgorithmsPhenotypeIn Situ Hybridization, FluorescenceGene Expression ProfilingAllelesHaplotypesGenetic LociModels, GeneticGenomic Structural VariationGenetics, PopulationGene DeletionDNA, MitochondrialGene FrequencyDatabases, GeneticDNAPolymorphism, GeneticHereditary Breast and Ovarian Cancer SyndromeGenotyping TechniquesMutationSoftwareEvolution, MolecularCase-Control StudiesChromosome DuplicationReproducibility of ResultsGenetic Association StudiesCluster AnalysisChromosomes, Human, Pair 1INDEL MutationPhylogenyChromosomes, MammalianChromosome DeletionComputational BiologyAsian Continental Ancestry GroupLinkage DisequilibriumChromosomes, Human, Pair 8ExomeGenes, NeoplasmMarkov Chains46, XX Disorders of Sex DevelopmentSpecies SpecificityHapMap ProjectHigh-Throughput Nucleotide SequencingKaryotypingChromosomes, Human, Pair 22ExonsChromosomes, Human, XLoss of HeterozygosityChromosomes, Human, Pair 16Autistic DisorderMicrosatellite RepeatsSequence DeletionGene Expression Regulation, NeoplasticReal-Time Polymerase Chain ReactionInheritance PatternsNucleic Acid Amplification TechniquesGenomic InstabilityChromosomes, Human, Pair 6Chromosomes, Human, Pair 2PedigreeEuropean Continental Ancestry GroupMicroarray AnalysisAneuploidyPseudogenesSelection, GeneticDNA Mutational AnalysisQuantitative Trait LociChromosomes, Human, Pair 20Chromosomes, Human, Pair 17RNA, MessengerPan troglodytesCell Line, TumorDNA, ViralDNA PrimersChromosomes